The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Protein zero (P0)–deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
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Citations
Cites
Rowland, L. P. (1993) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(12)62285-x · Cited by 581
Giese, K. P., Martini, R., Lemke, G., Soriano, P., & Schachner, M. (1992) · Cell · doi:10.1016/0092-8674(92)90591-y · Cited by 502
Self-citationMice deficient for the glycoprotein show subtle abnormalities in myelin
Montag, D., Giese, K. P., Bartsch, U., Martini, R., Lang, Y., Blüthmann, H., Karthigasan, J., Kirschner, D. A., Wintergerst, E. S., Nave, K.-A., et al. (1994) · Neuron · doi:10.1016/0896-6273(94)90472-3 · Cited by 377
Self-citationHypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
Adlkofer, K., Martini, R., Aguzzi, A., Zielasek, J., Toyka, K. V., & Suter, U. (1995) · Nature Genetics · doi:10.1038/ng1195-274 · Cited by 376
Self-citationCharcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
Hayasaka, K., Himoro, M., Sato, W., Takada, G., Uyemura, K., Shimizu, N., Bird, T. D., Conneally, P. M., & Chance, P. F. (1993) · Nature Genetics · doi:10.1038/ng0993-31 · Cited by 369
Crucial Role for the Myelin‐associated Glycoprotein in the Maintenance of Axon‐Myelin Integrity
Fruttiger, M., Montag, D., Schachner, M., & Martini, R. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00347.x · Cited by 231
Self-citationHusmann, K., Faissner, A., & Schachner, M. (1992) · The Journal of cell biology · doi:10.1083/jcb.116.6.1475 · Cited by 210
Self-citationHayasaka, K., Himoro, M., Sawaishi, Y., Nanao, K., Takahashi, T., Takada, G., Nicholson, G. A., Ouvrier, R. A., & Tachi, N. (1993) · Nature Genetics · doi:10.1038/ng1193-266 · Cited by 205
Kulkens, T., Bolhuis, P. A., Wolterman, R. A., Kemp, S., te Nijenhuis, S., Valentijn, L. J., Hensels, G. W., Jennekens, F. G. I., de Visser, M., Hoogendijk, J. E., et al. (1993) · Nature Genetics · doi:10.1038/ng0993-35 · Cited by 185
Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport
Gow, A., Friedrich, V. L., & Lazzarini, R. A. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490370504 · Cited by 159
Cited by
Disruption of the mouse L1 gene leads to malformations of the nervous system
Dahme, M., Bartsch, U., Martini, R., Anliker, B., Schachner, M., & Mantei, N. (1997) · Nature Genetics · doi:10.1038/ng1197-346 · Cited by 489
Self-citationMyelin synthesis in the peripheral nervous system
Garbay, B. (2000) · Progress in Neurobiology · doi:10.1016/s0301-0082(99)00049-0 · Cited by 314
EGR2 Mutations in Inherited Neuropathies Dominant-Negatively Inhibit Myelin Gene Expression
Nagarajan, R., Svaren, J., Le, N., Araki, T., Watson, M., & Milbrandt, J. (2001) · Neuron · doi:10.1016/s0896-6273(01)00282-3 · Cited by 273
Pennuto, M., Tinelli, E., Malaguti, M., Del Carro, U., D'Antonio, M., Ron, D., Quattrini, A., Feltri, M. L., & Wrabetz, L. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.021 · Cited by 265
On the molecular architecture of myelinated fibers
Arroyo, E. J., & Scherer, S. S. (2000) · Histochemistry and Cell Biology · doi:10.1007/s004180050001 · Cited by 252
Metadata
- Authors
- Martini, R., Zielasek, J., Toyka, K. V., Giese, K. P., & Schachner, M.
- Venue
- Nature Genetics
- Published
- 1995-11
- Volume
- 11
- Issue
- 3
- Pages
- 281-286
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2000053674
- Cited by
- 318
- References
- 22
- FWCI
- 6.86
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Protein zero (P0)–deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies. https://app.cochat.ai/papers/10.1038/ng1195-281
- The paper
- Martini, R., Zielasek, J., Toyka, K. V., Giese, K. P., & Schachner, M. (1995). Protein zero (P0)–deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies. Nature Genetics. https://doi.org/10.1038/ng1195-281
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
